US4318861AExpiredUtility

Stabilized diphenylmethane diisocyanate-polymethylene polyphenyl isocyanate compositions

Assignee: ATLANTIC RICHFIELD COPriority: Mar 18, 1981Filed: Mar 18, 1981Granted: Mar 9, 1982
Est. expiryMar 18, 2001(expired)· nominal 20-yr term from priority
C07C 263/18C08G 18/7664C08G 18/089
60
PatentIndex Score
6
Cited by
4
References
5
Claims

Abstract

Liquid reaction product mixtures of diphenylmethane diisocyanates and polymethylene polyphenyl isocyanates resulting from the thermal decomposition of the corresponding carbamates produced by the acid condensation of an N-aryl carbamic acid ester, such as ethylphenylcarbamate, with formaldehyde are storage stabilized against an increase in viscosity and decrease in free NCO content, by incorporating therein an effective amount of a compound having the formula ##STR1## wherein R is hydrogen or an alkyl group having up to 4 carbon atoms, x plus y is equal to 3 and z is an integer of from 0 to 3.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A method for the storage stabilization of liquid diphenylmethane diisocyanate-polymethylene polyphenyl isocyanate mixtures derived from the thermal decomposition of the corresponding diphenylmethane dicarbamates and polymethylene polyphenyl carbamates prepared by the acid condensation of N-aryl carbamic acid ester with formaldehyde, which comprises incorporating in said liquid isocyanate mixtures from about 0.001 to 1.0 percent by weight of an amide compound having the formula ##STR3## wherein R is hydrogen or an alkyl group having from 1 to 4 carbon atoms, x plus y is equal to 3 and z is an integer of from 0 to 3. 
     
     
       2. A method according to claim 1 wherein the amide compound is selected from the group consisting of N-(2-hydroxyethyl)trichloroacetamide, N-(2-hydroxypropyl)chlorobutramide, N-(2-hydroxybutyl)chloroacetamide, N-(2-hydroxybutyl)trichloropropamide, N-(2-hydroxyethyl)-2,2-dichloroacetamide and N-(2-hydroxyethyl)N-methyltrichloroacetamide. 
     
     
       3. A method according to claim 2 wherein the amide is N-(2-hydroxyethyl)trichloroacetamide. 
     
     
       4. A method according to claim 1 wherein the amide compound is employed in an amount of from 0.01 to 0.2 percent by weight. 
     
     
       5. A process according to claim 1 wherein the diphenylmethane diisocyanate content of the liquid isocyanate mixture is from about 20 to 85 weight percent.

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